1. Volume 38, Issue 3, Pages 570-580 (March 2013)
Inflammatory Monocytes Recruited to Allergic Skin Acquire an Anti-inflammatory M2 Phenotype via Basophil-Derived Interleukin-4 
Mayumi Egawa, Kaori Mukai, Soichiro Yoshikawa, Misako Iki, Naofumi Mukaida, Yohei Kawano, Yoshiyuki Minegishi, Hajime Karasuyama 
Immunity 
Volume 38, Issue 3, Pages (March 2013)
DOI: /j.immuni
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2. Immunity 2013 38, 570-580DOI: (10.1016/j.immuni.2012.11.014)
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3. Figure 1
Cellular Components in the IgE-CAI Reaction that Is Elicited by Basophils
(A) Mcpt8DTR C57BL/6 mice were sensitized with anti-TNP IgE and challenged with intradermal administration of TNP-OVA (or control OVA) in their ears to induce IgE-CAI. The mice were treated with either DT (open squares) or control PBS (closed squares) twice, 1 day before and 3 days after the antigen challenge. Time course of ear swelling (Δear thickness) is shown (mean ± SEM, n = 5 each). ∗p < 0.05, ∗∗∗p <
(B and C) C57BL/6 mice were sensitized with anti-TNP IgE and challenged with TNP-OVA (closed circles) or control OVA (open circles). The number of total cells (B) and indicated cell types (C) isolated from the ear skin at each time point postchallenge is shown (mean ± SEM, n = 3 each).
Data shown are representative of at least three independent experiments. Note that error bars are displayed in all figures, but often are hidden behind symbols such as squares and circles.
Immunity  , DOI: ( /j.immuni )
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4. Figure 2
Monocytes-Macrophages Accumulating in the IgE-CAI Skin Lesions Display a Phenotype of Inflammatory Monocytes
(A) C57BL/6 mice were treated as in Figure 1 to induce IgE-CAI. The expression of Ly6C and CCR2 on F4/80+CD11b+SSClo monocytes-macrophages in the skin lesions of mice challenged with TNP-OVA or control OVA was examined on day 4 postchallenge.
(B) The expression of CCR2 on indicated cell lineages isolated from the bone marrow of C57BL/6 and BALB/c mice. Shaded histograms show control staining with isotype-matched antibody.
(C) The expression of indicated mRNAs in the skin lesions of mice challenged with TNP-OVA or control OVA was examined on day 3 postchallenge (mean ± SEM, n = 5 each).
Data shown are representative of three independent experiments. NS, not significant; ∗∗p < See also Figures S1 and S2.
Immunity  , DOI: ( /j.immuni )
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5. Figure 3
IgE-CAI Is Exacerbated rather than Ameliorated in Ccr2−/− Mice
Wild-type and Ccr2−/− BALB/c mice were treated as in Figure 1 to induce IgE-CAI.
(A) Time course of ear swelling (Δear thickness) in wild-type (open squares) and Ccr2−/− (closed squares) mice is shown (mean ± SEM, n = 4–5 each). Note that error bars are displayed, but often are hidden behind symbols.
(B) Giemsa-stained specimens of IgE-CAI skin lesions isolated 4 days postchallenge.
(C) The numbers of total cells and indicated cell types isolated from the ear skin on day 4 postchallenge are shown (mean ± SEM, n = 4–5 each).
Data shown are representative of four independent experiments. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p <
Immunity  , DOI: ( /j.immuni )
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6. Figure 4
Monocytes-Macrophages Accumulating in the IgE-CAI Skin Lesions Display a Phenotype of M2-type Macrophages
(A–D) C57BL/6 mice were treated as in Figure 1 to induce IgE-CAI.
(A) The expression of PD-L2 on F4/80+CD11b+SSClo monocytes-macrophages in the skin lesions of mice challenged with TNP-OVA or control OVA was examined on day 4 postchallenge.
(B and C) Time course of the PD-L2+ monocytes-macrophage number (B, mean ± SEM, n = 3 each) and the expression of indicated mRNAs (C, mean ± SEM, n = 3 each) in the skin lesions of mice challenged with TNP-OVA (closed circles) or control OVA (open circles).
(D) The expression of indicated mRNAs in PD-L2− and PD-L2+ monocytes-macrophages that were isolated on day 3 postchallenge from the ear skin of mice challenged with TNP-OVA (mean ± SEM, n = 6 each).
(E) Wild-type and Ccr2−/− BALB/c mice were treated as in Figure 3 to induce IgE-CAI. Data show the numbers of PD-L2+ monocytes-macrophages that were isolated on day 4 postchallenge from the ear skin of mice challenged with TNP-OVA or control OVA (mean ± SEM, n = 4–5 each).
Data shown are representative of at least three independent experiments. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < See also Figures S1–S5.
Immunity  , DOI: ( /j.immuni )
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7. Figure 5
Basophil-Derived IL-4 Confers an M2-type Phenotype on Ly6C+ Inflammatory Monocytes Ex Vivo
(A and B) C57BL/6 mice were treated as in Figure 1 to induce IgE-CAI. Time course of the expression of indicated mRNAs in the skin lesions of mice challenged with TNP-OVA (closed circles) or control OVA (open circles) is shown in (A) (mean ± SEM, n = 3 each). ∗p < In (B), the indicated cell lineages were isolated on day 3 postchallenge from the skin lesions of mice challenged with TNP-OVA and subjected to quantitative RT-PCR for the analysis of Il4 expression (mean ± SEM, n = 3 each).
(C) Basophils (2 × 105 cells/ml) enriched from bone marrow cells were sensitized ex vivo with anti-TNP IgE and then stimulated with TNP-OVA or control OVA at 37°C for 10 hr, and the concentration of IL-4 and IL-13 in their culture supernatants was determined by ELISA (mean ± SEM, n = 5 each). ND, not detectable.
(D–F) Ly6C+ inflammatory monocytes were purified from C57BL/6 bone marrow cells and incubated at 37°C for 24 hr in the presence of anti-IL-4 or control rat IgG (rIgG), with the culture supernatants of basophils that had been stimulated as in (C).
(D and E) The cultured monocytes were subjected to flow cytometric analysis for PD-L2 expression. Representative staining profiles are shown in (D). Shaded histograms show control staining with isotype-matched antibody. All the data are summarized in (E) (mean ± SEM, n = 5–7 each), in that the relative mean fluorescence intensity (MFI) was calculated as MFI (PD-L2 staining)/MFI (control staining).
(F) The cultured monocytes were subjected to quantitative RT-PCR analysis for expression of indicated mRNAs (mean ± SEM, n = 5 each).
Data shown are representative of at least three independent experiments. ∗p < 0.05, ∗∗∗p <
Immunity  , DOI: ( /j.immuni )
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8. Figure 6
CD115+ Monocytes Acquire PD-L2 Expression after Their Infiltration into the Skin Lesions, in a Manner Dependent on IL-4R and Basophils
(A and B) CD115+ bone marrow cells isolated from BALB/c mice (A) or Ly6C+Ly6G− inflammatory monocytes (purity > 99%) sorted from CD115+ bone marrow cells (B) were labeled with CFSE and intravenously transferred (2 × 106 cells/mouse) into BALB/c mice that had been sensitized with anti-TNP IgE 1 day earlier. Recipient mice were challenged with intradermal administration of TNP-OVA immediately after the cell transfer. Flow cytometric analysis was performed for the surface expression of F4/80, PD-L2, and Ly6C in CFSE-labeled cells before the transfer and in those isolated from the TNP-OVA-injected skin on day 3 posttransfer.
(C) CD115+ bone marrow cells were prepared from wild-type or Il4ra−/− mice, labeled with CFSE, and intravenously transferred (3 × 106 cells/mouse) into IgE-sensitized BALB/c mice, followed by the antigen challenge (TNP-OVA or control OVA) as in (A) and (B). Flow cytometric analysis was performed for the surface expression of F4/80 and PD-L2 in CFSE-labeled cells before the transfer (left) and in those isolated from the ear skin on day 1 and day 3 posttransfer (middle and right, respectively).
(D) Mcpt8DTR C57BL/6 mice were sensitized with anti-TNP IgE and challenged with TNP-OVA as in Figure 1A to induce IgE-CAI. On day 2 postchallenge, the mice were treated with intravenous injection of CFSE-labeled CD115+ bone marrow cells (1 × 107 cells/mouse) derived from wild-type mice, in conjunction with DT or control PBS. On day 4 postchallenge, the expression of F4/80 and PD-L2 on CFSE-labeled cells isolated from the ear skin was examined.
Data shown are representative of three independent experiments.
Immunity  , DOI: ( /j.immuni )
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9. Figure 7
Adoptive Transfer of CCR2+Ly6C+ Inflammatory Monocytes from Wild-Type but Not Il4ra−/− Mice Normalizes the Exacerbated IgE-CAI in Ccr2−/− Mice
Ccr2−/− mice were treated as in Figure 3A to induce IgE-CAI.
(A) CD115+ (open squares) or CD115− (closed squares) bone marrow cells from BALB/c mice or control PBS (open triangles) were intravenously administered to the mice four times (1 × 106 cells/injection/mouse), on days 0, 1, 2, and 3 postchallenge. Time course of ear swelling (Δear thickness) is shown (mean ± SEM, n = 3–5 each).
(B) Ly6C+Ly6G− inflammatory monocytes (purity > 99%) sorted from bone marrow cells of wild-type (open squares) or Il4ra−/− (closed squares) mice were intradermally administered once (1 × 106 cells/site) in the ear of Ccr2−/− mice, in conjunction with administration of TNP-OVA or control OVA. Time course of ear swelling (Δear thickness) is shown (mean ± SEM, n = 4 each).
Data shown are representative of three independent experiments. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < Note that error bars are displayed in all figures, but often are hidden behind symbols. See also Figures S6.
Immunity  , DOI: ( /j.immuni )
Copyright © 2013 Elsevier Inc. Terms and Conditions